Faculty of Pharmacy, University of Coimbra, Pólo das Ciências da Saúde, Azinhaga de Santa Comba, 3000-548 Coimbra, Portugal.
Department of Food Science and Technology, University of the Peloponnese, 24100 Kalamata, Greece.
Nutrients. 2024 Jan 15;16(2):258. doi: 10.3390/nu16020258.
Sickle cell disease (SCD), a distinctive and often overlooked illness in the 21st century, is a congenital blood disorder characterized by considerable phenotypic diversity. It comprises a group of disorders, with sickle cell anemia (SCA) being the most prevalent and serious genotype. Although there have been some systematic reviews of global data, worldwide statistics regarding SCD prevalence, morbidity, and mortality remain scarce. In developed countries with a lower number of sickle cell patients, cutting-edge technologies have led to the development of new treatments. However, in developing settings where sickle cell disease (SCD) is more prevalent, medical management, rather than a cure, still relies on the use of hydroxyurea, blood transfusions, and analgesics. This is a disease that affects red blood cells, consequently affecting most organs in diverse manners. We discuss its etiology and the advent of new technologies, but the aim of this study is to understand the various types of nutrition-related studies involving individuals suffering from SCD, particularly in Africa. The interplay of the environment, food, gut microbiota, along with their respective genomes collectively known as the gut microbiome, and host metabolism is responsible for mediating host metabolic phenotypes and modulating gut microbiota. In addition, it serves the purpose of providing essential nutrients. Moreover, it engages in direct interactions with host homeostasis and the immune system, as well as indirect interactions via metabolites. Nutrition interventions and nutritional care are mechanisms for addressing increased nutrient expenditures and are important aspects of supportive management for patients with SCD. Underprivileged areas in Sub-Saharan Africa should be accompanied by efforts to define and promote of the nutritional aspects of SCD. Their importance is key to maintaining well-being and quality of life, especially because new technologies and products remain limited, while the use of native medicinal plant resources is acknowledged.
镰状细胞病(SCD)是一种在 21 世纪具有鲜明特征且经常被忽视的疾病,它是一种遗传性血液疾病,具有显著的表型多样性。它由一组疾病组成,其中镰状细胞贫血症(SCA)是最常见和最严重的基因型。尽管已经有一些关于全球数据的系统评价,但全球范围内关于 SCD 患病率、发病率和死亡率的统计数据仍然很少。在拥有较少镰状细胞患者的发达国家,先进的技术已经催生了新的治疗方法。然而,在镰状细胞病(SCD)更为普遍的发展中地区,医疗管理而非治愈,仍然依赖于使用羟基脲、输血和止痛药。这是一种影响红细胞的疾病,因此以不同的方式影响着大多数器官。我们讨论了它的病因和新技术的出现,但本研究的目的是了解涉及 SCD 患者的各种类型的与营养相关的研究,特别是在非洲。环境、食物、肠道微生物群及其各自的基因组(统称为肠道微生物群)以及宿主代谢之间的相互作用负责调节宿主代谢表型和调节肠道微生物群。此外,它还提供必需的营养物质。此外,它还与宿主内稳态和免疫系统直接相互作用,并通过代谢物间接相互作用。营养干预和营养护理是解决营养支出增加的机制,是 SCD 患者支持性管理的重要方面。撒哈拉以南非洲的贫困地区应努力确定和促进 SCD 的营养方面。这些方面对于维持健康和生活质量至关重要,特别是因为新技术和产品仍然有限,而本土药用植物资源的使用得到了认可。